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- CertificationWhatever the size of your company, wherever you are based, and whatever the category of your medical devices, we make it our mission to support you throughout your certification process.
- TrainingThe GMED North America Training Center delivers to you its expertise to enhance and develop your skills.
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- Focus on Medical DevicesTechnical and regulatory information in key medical device fields.
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- CompanyPresent in both Europe and North America, GMED’s level of excellence and standards have made it an internationally recognized name in the field of medical device certification.
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GMED Standard Rates

Applicable to services* in the framework of Regulation (EU) 2017/745 and Regulation (EU) 2017/746

SPECIFIC CONFORMITY ASSESSMENT ACTIVITIES	HOURLY RATE (Excluding VAT) Not included travel and management fees
Quality management system auditing	278 €
Assessment of the technical documentation	278 €
Clinical Evaluation	361 €
Evaluation of periodic safety update report [Article 86 of the Regulation (EU) 2017/745] [Article 81 of the Regulation (EU) 2017/746]	278 €
Validation of the Summary of safety and clinical performance [Article 32 of the Regulation (EU) 2017/745] Validation of the Summary of safety and performance [Article 29 of the Regulation (EU) 2017/746]	278 €

*Applicable rates for activities managed by our European offices